Maquet Cardiovascular, LLC: Medical Device Recall in 2023 - (Recall #: Z-0210-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Vasoview 6 Pro (VV6) - Endoscopic Vessel Harvesting System, Model VH-2400 printed on outer label, inner label and IFU, outer box artwork for Vasoview Hemopro 2 (HP2).

Product Classification:

Class II

Date Initiated: September 19, 2023

Date Posted: November 8, 2023

Recall Number: Z-0210-2024

Event ID: 93297

Reason for Recall:

Device packaged inside an incorrect outer box; displaying artwork & illustrations for a different device.

Status: Ongoing

Product Quantity: N/A

Code Information:

UDI-DI: 00607567700239, Lot: 3000313857.

Distribution Pattern:

US (AL, AR, CA, FL, GA, IN, KY, MI, NJ, OK, PA, TN, TX) and Canada.

Voluntary or Mandated:

Voluntary: Firm initiated